Different role of insulin in GLUT-1 and -4 regulation in heart and skeletal muscle during perinatal hypothyroidism

Am J Physiol Endocrinol Metab. 2001 Nov;281(5):E1073-81. doi: 10.1152/ajpendo.2001.281.5.E1073.

Abstract

Two groups of hypothyroid rats were used; one group was given 2-mercapto-1-methylimidazole (MMI) treatment in the drinking water of the mothers and was killed at 2 and 4 days of life, and the other group was given similar MMI treatment and then was thyroidectomized at 5 days of life and killed at 8 or 20 days. Serum insulin, growth hormone (GH), and insulin-like growth factor I (IGF-I) were decreased in MMI-treated rats but increased in MMI-treated plus thyroidectomized rats. No significant reduction of thyroid hormones was observed in 2-day-old MMI rats. Protein and mRNA expression of GLUT-1 increased, and those of GLUT-4 decreased, in the heart in all populations independent of changes in insulin, GH, and IGF-I levels. However, GLUT-4 protein and mRNA expression in quadriceps and gastrocnemius skeletal muscles decreased at 4 days and increased at 8 and 20 days of life in parallel with insulin, GH, and IGF-I levels. GLUT-1 in the skeletal muscles seemed regulated posttranscriptionally and presented a decrease of mRNA expression in all stages studied. A differential sensitivity to insulin regulation of GLUT-1 and GLUT-4 glucose transporters seems to be one of the causes for the tissue-specific regulation of these glucose transporters in heart and skeletal muscles during the perinatal period.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Female
  • Gene Expression
  • Gestational Age
  • Glucose Transporter Type 1
  • Glucose Transporter Type 4
  • Growth Hormone / blood
  • Hypothyroidism / chemically induced
  • Hypothyroidism / metabolism*
  • Insulin / blood
  • Insulin / physiology*
  • Insulin-Like Growth Factor I / analysis
  • Liver / chemistry
  • Maternal-Fetal Exchange
  • Methimazole / administration & dosage
  • Monosaccharide Transport Proteins / genetics
  • Monosaccharide Transport Proteins / metabolism*
  • Muscle Proteins*
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / metabolism*
  • Myocardium / chemistry
  • Myocardium / metabolism*
  • Pregnancy
  • RNA, Messenger / analysis
  • Rats
  • Rats, Wistar
  • Thyroidectomy

Substances

  • Glucose Transporter Type 1
  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • RNA, Messenger
  • Slc2a1 protein, rat
  • Slc2a4 protein, rat
  • Methimazole
  • Insulin-Like Growth Factor I
  • Growth Hormone